Environmental Monitoring and Sampling Technician
Puerto Rico
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Environmental Monitoring and Sampling Technician
PR, Juncos, Puerto Rico
Full Time
Entry Level
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Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto Rico, and Boston, United States, we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America. Under general supervision, the Environmental Monitoring and Sampling Coordinator will perform routine procedures and sampling of environmental monitoring, water systems, and gases in support of Manufacturing Operations; plans and prepare the team schedule to achieve a High Performing Team environment; among other tasks.Responsibilities: Under general supervision, this position will perform routine procedures and sampling of environmental monitoring, water systems and gases in support of Manufacturing operations.Complete logs and reports as required.Reviewing shift personnel vs. capacity requirements to run the sampling process as per the scheduled plan. Plans and organizes the area work to achieve a High Performing Team environment.Ensures that work performed by area team members is accurate, timely, efficient and compliant with corporate policies, SOPs, cGMP regulations, and regulatory agencies regulations (FDA, EMEA).Assures a streamlined and continuous process flow of environmental monitoring and sampling area.Perform environmental monitoring routine sample collection, sample receipt, sample incubation, and downstream results analysis, interpretation, and reporting, according to the SOP’s.Will also be responsible for documenting and entering data into applicable GMP forms.Must learn and comply with safety guidelines, GLP, and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, written procedures and logbooks.Ensure timely completion of testing and tasks as assigned (support).Identify opportunities for continuous improvements.Maintain instrumentation and equipment preventative maintenance and supporting documentation in a cGMP compliant manner.Assist in the implementation of new assay methodologies and the associated instrumentation.Identify and support initiation of Deviations, CAPAs and Laboratory Investigations, as required by the client sponsor and as indicated in established procedures.Determines team schedule, updates schedule’s board, communicates daily schedule performance to team members and communicates the shift production information with other shifts supervisor or manager.Provides input in the creation and revision of SOP’s, protocols, and related documents to assure compliance with cGMP’s, company policies / procedures and documentation practices.Provides support to the area environmental monitoring and sampling reports. Monitors, evaluates and communicates area performance metrics for processes, cost and quality.Maintains accurate tracking records and provides timely feedback to supervisor regarding status of assigned area/tasks.Provides, in coordination with other departments, the guidance and resources to support validation projects, troubleshooting, lots of production, and process optimization.Ensures the application of cGMP compliance with respect to the Team, shop floor and documentation. Review area documentation to ensure it is complete, accurate, error free, and on time delivery.Follow the Puerto Rico Department of Transportation...